4-(2-(Trifluoromethyl)phenoxy)benzenesulfonylchloride CAS 885950-91-4

Purity 97%+In StockPharmaceutical Standards
CAS No.885950-91-4
Molecular FormulaC13H8ClF3O3S
Molecular Weight336.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2-(Trifluoromethyl)phenoxy)benzenesulfonylchloride CAS 885950-91-4 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

4-(2-(Trifluoromethyl)phenoxy)benzenesulfonylchloride (CAS 885950-91-4), molecular formula C13H8ClF3O3S and molecular weight 336.71 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C13H8ClF3O3S, 4-(2-(Trifluoromethyl)phenoxy)benzenesulfonylchloride contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 336.71 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 4-(2-(Trifluoromethyl)phenoxy)benzenesulfonylchloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H8ClF3O3S
Molecular Weight336.71 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Sulfur Atoms1

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